Canonical Allele Identifier: CA2839791
Gene: WFS1 HGNC NCBI

Linked Data

dbSNP Id: rs778180190
gnomAD v2: 4-6304106-A-T
gnomAD v3: 4-6302379-A-T
gnomAD v4: 4-6302379-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6302379A>T , CM000666.2:g.6302379A>T GRCh38
NC_000004.11:g.6304106A>T , CM000666.1:g.6304106A>T GRCh37
NC_000004.10:g.6355007A>T NCBI36
NG_011700.1:g.37530A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000682275.1:c.2620A>T ENSP00000507852.1:p.Lys874Ter
ENST00000683395.1:c.2561A>T
ENST00000684087.1:c.2584A>T ENSP00000506978.1:p.Lys862Ter
ENST00000506362.2:c.2335A>T ENSP00000424103.2:p.Lys779Ter
ENST00000673991.1:c.2620A>T ENSP00000501033.1:p.Lys874Ter
ENST00000226760.5:c.2584A>T MANE Select ENSP00000226760.1:p.Lys862Ter
ENST00000503569.5:c.2584A>T ENSP00000423337.1:p.Lys862Ter
ENST00000507765.1:n.2769A>T
NM_001145853.1:c.2584A>T NP_001139325.1:p.Lys862Ter
NM_006005.3:c.2584A>T MANE Select NP_005996.2:p.Lys862Ter
XM_017008586.1:c.2593A>T XP_016864075.1:p.Lys865Ter